445018-45-1

Upstream product

• 445018-43-9 tert-butyl (3R,αS)-3-(N-benzyl-N-α-methyl-4-methoxybenzylamino)pent-4-enoate 
• 160460-40-2 [(S)-1-(4-Methoxy-phenyl)-ethyl]-[1-phenyl-meth-(E)-ylidene]-amine 
• 120343-46-6 (S)-N-benzyl-N-(α-methyl-p-methoxybenzyl)amine 
• 6298-96-0 (S)-1-(4-methoxyphenyl)ethylamine 
• 445018-44-0 tert-butyl (3R,αS)-3-(N-α-methyl-4-methoxybenzylamino)pent-4-enoate 

Downstream Products

• 445018-46-2 (4R,αS)-N-(α-methyl-4-methoxybenzyl)-4-vinylazetidin-2-one 

Relevant academic research and scientific papers

Orthogonal N,N-deprotection strategies of β-amino esters

β-Amino esters derived from the stereoselective conjugate addition of homochiral lithium N-benzyl-N-α-methyl-4-methoxybenzylamide to α,β-unsaturated esters may be orthogonally mono-N-deprotected under either oxidative or acid-promoted reaction conditions. Further oxidative deprotection affordsβ-amino acids or β-lactams.